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FDA 510(k)

50 DEGREE HRI PRISM LENS

K-Number: K941420 · 1994-08-29

Decision Date1994-08-29
Product CodeHJK
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

50 DEGREE HRI PRISM LENS is the device name listed in this FDA 510(k) record. The listed applicant is Ocular Instruments, Inc.. It received FDA 510(k) clearance on 1994-08-29 under 510(k) number K941420. The device is classified under product code HJK. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 50 DEGREE HRI PRISM LENS?

50 DEGREE HRI PRISM LENS is a medical device that received FDA 510(k) clearance on 1994-08-29. The listed applicant is Ocular Instruments, Inc.. The 510(k) number is K941420.

When did 50 DEGREE HRI PRISM LENS receive FDA 510(k) clearance?

50 DEGREE HRI PRISM LENS received FDA 510(k) clearance on 1994-08-29, under 510(k) number K941420.

Who is the listed applicant for 50 DEGREE HRI PRISM LENS?

The FDA 510(k) record lists Ocular Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 50 DEGREE HRI PRISM LENS?

The FDA product code for 50 DEGREE HRI PRISM LENS is HJK.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Ocular Instruments, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: HJK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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